FDA UDI In Commercial Distribution 🇺🇸 United States

CHS

DI: 03596010175137 · Model: 71123196 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CHS
Primary DI
03596010175137
Version / Model
71123196
Catalog Number
71123196
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-25
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
343b0526-08e0-44ba-a4cd-7f6e2c6f90f9

Device Description

INTERMEDIATE LAG SCREW 85MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 03596010175137

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K993289 000